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2-Methyl-4-nitrophenol → 1-(Difluoromethoxy)-2-methyl-4-nitrobenzene

HRID 2110136
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HRID 2110136 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:11].C([O-])([O-])=O.[Cs+].[Cs+].Cl[C:19]([F:24])([F:23])C([O-])=O.[Na+]>CN(C)C=O.O>[F:23][CH:19]([F:24])[O:11][C:3]1[CH:4]=[CH:5][C:6]([N+:8]([O-:10])=[O:9])=[CH:7][C:2]=1[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 74422-Methyl-4-nitrophenolHCID 10796Cesium carbonateHCID 2734985Sodium chlorodifluoroacetate

생성물 1

HCID 133147061-(Difluoromethoxy)-2-methyl-4-nitrobenzene수율 86.1%

시약·촉매·용매 2

HCID 962Water용매2회HCID 6228
Dimethylformamide
용매

실험 절차

To a solution of 2-methyl-4-nitrophenol (14 g, 91.50 mmol) in dimethylformamide (120 mL) and water (25 mL) was added Cs2CO3 (41.8 g, 128.22 mmol), and sodium 2-chloro-2,2-difluoroacetate (32 g, 209.84 mmol). The resulting solution was stirred for 20 minutes at room temperature, then for an additional 3 hours at 100° C. The reaction solution was cooled to room temperature before the addition of 100 ml of H2O. The resulting solution was extracted with EtOAc (4×100 ml) and the combined organic layers were washed with H2O (2×150 mL), dried over Na2SO4, concentrated in vacuo. The residue was purified by silica gel column chromatography to provide 16 g (86%) of 1-(difluoromethoxy)-2-methyl-4-nitrobenzene.

후처리

  1. waitfor an additional 3 hours at 100° C
  2. extractionThe resulting solution was extracted with EtOAc (4×100 ml)
  3. washthe combined organic layers were washed with H2O (2×150 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-ab4986c9cc964a6591c75f506284d803
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07517884B2

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